ENST00000703936.1:c.2806G>C
|
ENSP00000515567.1:p.Asp936His
|
|
ENST00000703937.1:c.*1867G>C
|
ENSP00000515568.1:n.*1867G>C
|
|
ENST00000326739.9:c.766G>C
MANE Select
|
ENSP00000321584.4:p.Asp256His
|
|
ENST00000429182.6:c.766G>C
|
ENSP00000393525.2:p.Asp256His
|
|
ENST00000442157.2:c.691G>C
|
ENSP00000403502.2:p.Asp231His
|
|
ENST00000462980.2:n.1281G>C
|
|
|
ENST00000472328.2:n.832G>C
|
|
|
ENST00000491610.2:n.726G>C
|
|
|
ENST00000676607.1:n.1062G>C
|
|
|
ENST00000676627.1:n.1496G>C
|
|
|
ENST00000676708.1:n.2046G>C
|
|
|
ENST00000676864.1:n.1915G>C
|
|
|
ENST00000677010.1:c.802G>C
|
ENSP00000503089.1:p.Asp268His
|
|
ENST00000677108.1:n.2672G>C
|
|
|
ENST00000677168.1:n.1238G>C
|
|
|
ENST00000677185.1:n.1329G>C
|
|
|
ENST00000677205.1:n.1550G>C
|
|
|
ENST00000677344.1:n.2040G>C
|
|
|
ENST00000677480.1:c.*443G>C
|
ENSP00000504378.1:n.*443G>C
|
|
ENST00000677519.1:n.1476G>C
|
|
|
ENST00000677593.1:n.1322G>C
|
|
|
ENST00000677740.1:n.2271G>C
|
|
|
ENST00000677991.1:n.1939G>C
|
|
|
ENST00000678001.1:n.1259G>C
|
|
|
ENST00000678085.1:n.1322G>C
|
|
|
ENST00000678177.1:n.2615G>C
|
|
|
ENST00000678603.1:n.1844G>C
|
|
|
ENST00000678724.1:c.691G>C
|
ENSP00000503874.1:p.Asp231His
|
|
ENST00000678920.1:n.924G>C
|
|
|
ENST00000679019.1:n.1536G>C
|
|
|
ENST00000679117.1:c.*581G>C
|
ENSP00000503240.1:n.*581G>C
|
|
ENST00000679339.1:n.1607G>C
|
|
|
ENST00000326739.8:c.766G>C
|
ENSP00000321584.4:p.Asp256His
|
|
ENST00000429182.5:c.560G>C
|
|
|
ENST00000442157.1:c.691G>C
|
ENSP00000403502.1:p.Asp231His
|
|
ENST00000462980.1:n.668G>C
|
|
|
ENST00000491610.1:n.726G>C
|
|
|
NM_000884.2:c.766G>C
|
NP_000875.2:p.Asp256His
|
|
XM_006713128.2:c.976G>C
|
XP_006713191.1:p.Asp326His
|
|
XM_006713128.3:c.976G>C
|
XP_006713191.1:p.Asp326His
|
|
XM_017006349.1:c.901G>C
|
XP_016861838.1:p.Asp301His
|
|
XM_017006350.1:c.901G>C
|
XP_016861839.1:p.Asp301His
|
|
NM_000884.3:c.766G>C
MANE Select
|
NP_000875.2:p.Asp256His
|
|